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Threshold Pedicular Fixation System, Palisade Pedicular Fixation System

K160980 Class II Special
Decision Date
2016-05-26
Sponsor / Applicant
Spineology, Inc.

Technical Specification

510(k) Submission ID K160980
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2016-05-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Threshold Pedicular Fixation System, Palisade Pedicular Fixation System received FDA 510(k) clearance under submission number K160980, sponsored by Spineology, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.